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. 2021 Feb 17;1(3):100043. doi: 10.1016/j.phyplu.2021.100043

Table 1.

Antiviral activity and mechanism of action of licorice extract in articles published from 2006 to 2020.

Extract Method of research Major finding Mechanism of actions References
Licorice extract
95% ethanol extract of Glycyrrhiza ‘uralensis’
H1N1infected human bronchial epithelial cells (A549). Inhibition of  influenza A virus (H1N1). Inhibit RANTES secretion. Ko et al., 2006.

Licorice extract Randomized controlled trials Reduced hepatocellular damage in chronic hepatitis B and C. Reduced transport to the membrane. Fiore et al., 2008.

Aqueous extract of  Glycyrrhiza uralensis. Human foreskin fibroblast cell line. Inhibited enterovirus 71. By preventing viral attachment and penetration. Kuo et al., 2009.

Hot water extracts of licorice Human Respiratory Tract Cell Lines. Anti-Viral Activity Against Human Respiratory Syncytial Virus. Aquous ext., are highly  effective against HRSV infection on airway epithelial cells. By preventing viral attachment, internalization, and by stimulating IFN secretion. Feng et al., 2013

Licorice extract HCV cell culture system. It has anti-HCV  more than  glycyrrhizin. Unknown Adianti et al., 2014

Licorice extract Cell line Superiority of alkaline extraction over water extraction  as anti-HIV. Unknown Ohno et al., 2014

Licorice extract  rich Oleanane-Type Triterpene Saponins MDCK cells Inhibit many virus. Inhibition of neuraminidase. Wei et al., 2014

Licorice extract rich oleanane-type triterpenoid saponins. Cell line In vitro anti-influenza virus activity comparable to and even higher than that of oseltamivir. Suppression of virus release by GL treatment may be due to its inhibitory effect on PLA2G1B. Song et al., 2014

Alkanine extract & water  extract of licorice root Cells line Alkaline extract  was highly effective against HIV  and more than aquous extract. While aquous extract was more effective against
HSV-infected cells.
Unknown Fukuchi et al., 2016

Licorice extract and bioactive ingredients Molecular Docking and ADMET Study Inhibitor  SARS-CoV2 while Gl  better ADMET. Potential to be strong inhibitors for Main protease  of SARS-CoV2. Srivastava et al., 2020